Kouri Maria, Papadopoulou Erofili, Vardas Emmanouil, Georgaki Maria, Rekatsina Martina, Tsaroucha Athanasia, Pasqualucci Alberto, Vadalouca Athina, Varrassi Giustino, Nikitakis Nikolaos G
Anesthesiology, National and Kapodistrian University of Athens, Athens, GRC.
Oral Medicine and Pathology and Hospital Dentistry, School of Dentistry, National and Kapodistrian University of Athens, Athens, GRC.
Cureus. 2024 Nov 3;16(11):e72951. doi: 10.7759/cureus.72951. eCollection 2024 Nov.
Head and neck cancer (HNC) patients may experience neuropathic pain (NP) due to radiotherapy (RT), which may become chronic. Pregabalin, an anticonvulsant, alters the transmission of painful stimuli at the synaptic level, modifying their perception. Pregabalin is used in NP treatment, but limited data exist on RT-treated HNC patients. This retrospective study aimed to present a case series of HNC patients with chronic NP after RT managed with pregabalin.
HNC patients' records from the Department of Oral Medicine and Pathology and Hospital Dentistry, School of Dentistry, National and Kapodistrian University of Athens (NKUA), were searched. Outcome measures were obtained using the Douleur Neuropathique 4 (DN4) scale for NP and the numeric rating scale (NRS) for pain. The use of additional analgesic medication was also recorded.
Five HNC (four oral and one nasopharyngeal cancer) patients (mean age 58.5 years) who had received RT (mean total dose 64.7 gray (Gy)) and developed chronic (i.e., present for at least three months after RT) NP, characterized by a positive DN4 score ≥4, were identified. The initial assessment was five months to six years after RT (mean DN4=4.6±0.89 and mean NRS=6±3.08). "Burning," "pins and needles," and "numbness" were the NP descriptors mostly used. Pregabalin was titrated up to 150-300 mg per day; paracetamol and/or tramadol were also administered (daily doses 3000 mg and 100-150 mg, respectively). A substantial pain relief (≥50%) according to the Initiative on Methods, Measurement, and Pain Assessment in Clinical Trials (IMMPACT) (mean DN4=1.6±1.67 and NRS=1.6±1.67) was reported after two to three months of treatment, when tapering was initiated. Two patients (2/5) had complete remission of symptoms (DN4=0, NRS=0). No serious adverse effects were reported; one patient reported excess salivation.
Pregabalin may be a promising option for managing RT-related chronic NP in HNC patients. Further studies, including randomized controlled trials on RT-treated HNC patients, should be conducted.
头颈癌(HNC)患者可能因放疗(RT)而经历神经性疼痛(NP),这种疼痛可能会变为慢性疼痛。普瑞巴林是一种抗惊厥药,可在突触水平改变疼痛刺激的传递,从而改变患者对疼痛的感知。普瑞巴林用于治疗NP,但关于接受放疗的HNC患者的数据有限。这项回顾性研究旨在呈现一组接受普瑞巴林治疗的放疗后出现慢性NP的HNC患者病例系列。
检索了雅典国立与卡波迪斯特里亚大学(NKUA)牙科学院口腔医学与病理学系及医院牙科的HNC患者记录。使用用于NP的神经病理性疼痛4(DN4)量表和用于疼痛的数字评分量表(NRS)来获取结果指标。还记录了额外镇痛药物的使用情况。
确定了5例HNC患者(4例口腔癌和1例鼻咽癌)(平均年龄58.5岁),他们接受了放疗(平均总剂量64.7戈瑞(Gy))并出现了慢性(即放疗后至少持续三个月)NP,其特征为DN4评分≥4呈阳性。初始评估在放疗后5个月至6年进行(平均DN4 = 4.6±0.89,平均NRS = 6±3.08)。“灼痛”“刺痛”和“麻木”是最常使用的NP描述词。普瑞巴林的剂量逐渐增加至每日150 - 300毫克;还给予了对乙酰氨基酚和/或曲马多(每日剂量分别为3000毫克和100 - 150毫克)。根据临床试验中的方法、测量和疼痛评估倡议(IMMPACT),在治疗两到三个月后开始减药时,报告疼痛有显著缓解(≥50%)(平均DN4 = 1.6±1.67,NRS = 1.6±1.67)。两名患者(2/5)症状完全缓解(DN4 = 0,NRS = 0)。未报告严重不良反应;一名患者报告有唾液分泌过多的情况。
普瑞巴林可能是治疗HNC患者放疗相关慢性NP的一个有前景的选择。应开展进一步研究,包括针对接受放疗的HNC患者的随机对照试验。